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Data updated: Mar 10, 2026

BEPREVE

BEPOTASTINE BESILATE
Ophthalmology Approved 2009-09-08
1
Indication
--
Phase 3 Trials
16
Years on Market

Details

Status
Prescription
First Approved
2009-09-08
Routes
OPHTHALMIC
Dosage Forms
SOLUTION/DROPS

Companies

Active Ingredient: BEPOTASTINE BESILATE

BEPREVE Approval History

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What BEPREVE Treats

1 indications

BEPREVE is approved for 1 conditions since its original approval in 2009. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Allergic Conjunctivitis
Source: FDA Label

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Active Pipeline

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Ongoing clinical trials by development phase

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Key Completed Trials

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Completed studies with published results, ranked by significance

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Trial Timeline

Full development history with FDA approval milestones

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Understanding FDA Approval Types
Count Type What it means
- ORIG Original approval - drug first enters market
- SUPPL - Efficacy New indication (new disease/condition approved)
- SUPPL - Labeling Label text changes (warnings, dosing updates)
- SUPPL - Manufacturing Production changes (new facility)
- SUPPL - Chemistry Formulation changes (new dosage strength)

Green lines in the timeline show ORIG and Efficacy approvals - the clinically meaningful milestones.

BEPREVE FDA Label Details

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Indications & Usage

FDA Label (PDF)

BEPREVE ® (bepotastine besilate ophthalmic solution) 1.5% is a histamine H 1 receptor antagonist indicated for the treatment of itching associated with signs and symptoms of allergic conjunctivitis. BEPREVE is a histamine H1 receptor antagonist indicated for the treatment of itching associated with allergic conjunctivitis.

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Data Sources

Data sourced from official FDA and NIH databases. Click links to verify on original sources.